A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459859



Internal ID21117412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:90406680..90415974hg38UCSC Ensembl
chr12:90800457..90809751hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg389295
hg199295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18004956
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459859
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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